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Rotator Cuff Tears clinical trials

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NCT ID: NCT04703998 Completed - Rotator Cuff Tears Clinical Trials

Arthroscopic Rotator Cuff Repair Augmented With Platelet Rich Plasma

Start date: January 3, 2021
Phase: N/A
Study type: Interventional

Purpose: To assess whether the use of platelet-rich plasma used as an adjuvant to arthroscopic rotator cuff repairs modify the rate of re-tears (measured by MRI) compared to a control group that only underwent the isolated arthroscopic repair. Hypothesis: Platelet rich plasma used as an adjuvant to arthroscopic rotator cuff repairs decrease the rate of retears.

NCT ID: NCT04692649 Completed - Shoulder Pain Clinical Trials

Comparison of Pragmatic Posterior Capsular Stretch and Crossbody Stretch on the Shoulder Mobility

Start date: January 5, 2021
Phase: N/A
Study type: Interventional

Various stretches are used to lengthen the posterior shoulder capsule. No study has reported the comparison of the pragmatic posterior capsular stretch and cross body stertch

NCT ID: NCT04628676 Completed - Rotator Cuff Tears Clinical Trials

Comparison of the Efficacy of Irrigation With Epinephrine or Tranexamic Acid on Visual Clarity

Start date: February 1, 2017
Phase: N/A
Study type: Interventional

The primary aim of this report is to determine whether there is a difference between Epinephrine and Tranexamic acid in providing visual clarity during arthroscopic rotator cuff tear repair.

NCT ID: NCT04594408 Completed - Rotator Cuff Tears Clinical Trials

Tranexamic Acid to Improve Arthroscopic Visualization in Shoulder Surgery

Start date: September 1, 2020
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine if intravenous TXA is a safe alternative to epinephrine in improving arthroscopic shoulder visualization. Primary Objectives 1. Determine that patients given intravenous tranexamic acid improves surgeon-rated visualization compared to placebo. 2. Determine that intravenous tranexamic acid is a safe alternative to epinephrine mixed irrigation fluid to improve arthroscopic shoulder visualization

NCT ID: NCT04593342 Completed - Rotator Cuff Tears Clinical Trials

Photobiomodulation Laser Therapy Following Arthroscopic Rotator Cuff Repair

LLL&RotC01
Start date: November 26, 2020
Phase: N/A
Study type: Interventional

Rehabilitation following rotator cuff surgery is characterized with high levels of pain, limited range of motion, and decreased quality of life. The purpose of this study is to evaluate the B-Cure laser photobiomodulation home-use device in addition to standard care, for the reduction of pain, increase in functionality, and improvement of life quality during rehabilitation following rotator cuff arthroscopic surgery.

NCT ID: NCT04587180 Completed - Rotator Cuff Tears Clinical Trials

Cutting-through at the Greater Tuberosity

Start date: June 1, 2014
Phase:
Study type: Observational

The investigators evaluated the correlation between cutting-through at the greater tuberosity (GT) just medial to the lateral knotless anchor in arthroscopic suture-bridge rotator cuff repair and the bone mineral density (BMD) of the lumbar spine, hip and GT of the proximal humerus and to evaluate factors and clinical outcomes related to cutting-through at the GT.

NCT ID: NCT04552925 Completed - Rotator Cuff Tears Clinical Trials

Exercises With Electromyographic Biofeedback in Conservative Treatment of Massive Rotator Cuff Tears

Start date: September 22, 2020
Phase: N/A
Study type: Interventional

There are very few studies in the literature about conservative treatment of massive rotator cuff (RC) tears. Whether the treatment of massive RC tears is conservative or surgical is decided according to the age, activity level, expectation and additional pathologies of the patient. The aim of conservative treatment is to make the patient functionally independent and to reduce pain. In recent years, there are different opinions in the literature about the effectiveness of conservative treatment of massive RC tears. However, in recent biomechanical studies, it has been reported that the RC and the deltoid, which remain intact in massive RC tears, can function well together. The hypothesis of this study is that the deltoid-focused physiotherapy program, where strengthening exercises are performed with EMG biofeedback, will give more positive results in terms of range of motion (ROM), functional status, muscle strength, pain and patients satisfaction. aim of our study is to investigate the efficacy of electromyographic biofeedback (EMG-BF) device which was added to deltoid focused conservative treatment program in massive RC tears.

NCT ID: NCT04538118 Completed - Rotator Cuff Tears Clinical Trials

Relationship of Patient-Specific Functional Scale With Shoulder Functions: A Prospective Study

Start date: January 5, 2019
Phase:
Study type: Observational [Patient Registry]

The aim of the study is to examine the relationship between the Patient- Specific Functional Scale (PSFS) and shoulder functions in the physiotherapy and rehabilitation program applied to patients with shoulder problems.

NCT ID: NCT04521504 Completed - Rotator Cuff Tears Clinical Trials

The ISEO Biofeedback Tool During the Rehabilitation of Patients Treated for Rotator Cuff Tear

PDT1-1
Start date: November 21, 2017
Phase: N/A
Study type: Interventional

The present study addresses the issue about post-surgical recovery process, for patients arthroscopically treated for rotator-cuff tear. The aim of the research is to test the effectiveness of a new rehabilitation protocol that includes kinematic biofeedback with the motion analysis system ISEO.

NCT ID: NCT04470570 Completed - Rotator Cuff Tears Clinical Trials

The Effect of Cross-Education on Shoulder Arthroscopy

Start date: July 13, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to examine the effectiveness of a strength training protocol on the uninjured upper extremity either alone or with the addition of blood flow restriction (BFR) training on subjects who have undergone shoulder arthroscopy.